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'Role reversal' for the receptor PAR1 in sepsis-induced vascular damage

2007; Nature Portfolio; Volume: 8; Issue: 12 Linguagem: Inglês

10.1038/ni1525

1529-2916

Nicole C. Kaneider, Andrew J. Leger, Anika Agarwal, Nga Nguyen, George Perides, Claudia K. Derian, Lidija Covic, Athan Kuliopulos,

S100 Proteins and Annexins

This is an Issue edsumm for 934. Identification of the Palaeocene/Eocene thermal maximum in a marine sedimentary sequence shows that sea surface temperatures near the North Pole increased from roughly 18 degrees Celsius to over 23 degrees Celsius — such warm values imply the absence of ice and thus exclude the influence of ice-albedo feedbacks on this Arctic warming. Sepsis is a deadly disease characterized by considerable derangement of the proinflammatory, anti-inflammatory and coagulation responses. Protease-activated receptor 1 (PAR1), an important regulator of endothelial barrier function and blood coagulation, has been proposed to be involved in the lethal sequelae of sepsis, but it is unknown whether activation of PAR1 is beneficial or harmful. Using a cell-penetrating peptide (pepducin) approach, we provide evidence that PAR1 switched from being a vascular-disruptive receptor to a vascular-protective receptor during the progression of sepsis in mice. Unexpectedly, we found that the protective effects of PAR1 required transactivation of PAR2 signaling pathways. Our results suggest therapeutics that selectively activate PAR1-PAR2 complexes may be beneficial in the treatment of sepsis.